• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

苏丹镰状细胞病患者稳定期与血管阻塞危象期高凝状态变化的对比研究。

Comparative study of hypercoagulability change in steady state and during vaso-occlusive crisis among Sudanese patients living with sickle cell disease.

机构信息

Alghad International Colleges for Applied Medical Sciences, Educational and Academic Affairs.

Taibah university, college of Applied Medical science, Medical Laboratory Science.

出版信息

Afr Health Sci. 2020 Mar;20(1):392-396. doi: 10.4314/ahs.v20i1.45.

DOI:10.4314/ahs.v20i1.45
PMID:33402927
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7750086/
Abstract

BACKGROUND

Sickle cell disease (SCD) is an inherited blood disorder that affects red blood cells. (SCD) is characterized by recurrent vaso-occlusive crisis (VOC).

MATERIAL AND METHODS

This was a descriptive cross sectional study conducted through the period from July 2015 to July 2017 in which a total of seventy two blood specimens were collected in 'EDTA' and citrated vacutainers from Sudanese patients with SCD attending "Fath Elrhman Albasheer" Centre. Both sexes' with different ages were included. Among these samples 49 (68.1%) were in steady state while the remained 23 (31.9%) were in VOC. All samples were tested for coagulation profile.

RESULT

There was increase in fibrinogen and D-dimer levels in most patients 67% and 71%, respectively. Significant increase in D-dimers was observed in patients with (VOC) compared with steady state (P. value = 0.006). Protein S was significantly increased in males in comparison with females P. value = 0.017. The results of prothrombin time (PT), international normalized ratio (INR) and thrombin time (TT) were within normal range.

CONCLUSION

Significant increase in levels of D-dimer during VOC indicating abnormal coagulation and fibrinolysis activation. Reduced levels of natural anticoagulants proteins C and S can be consider as predictive markers indicate hepatic dysfunction in patients with SCD.

摘要

背景

镰状细胞病(SCD)是一种遗传性血液病,影响红细胞。(SCD)的特征是反复发作的血管阻塞性危象(VOC)。

材料和方法

这是一项描述性的横断面研究,于 2015 年 7 月至 2017 年 7 月期间进行,共从苏丹 SCD 患者在“Fath Elrhman Albasheer”中心采集了 72 份 EDTA 和枸橼酸盐真空采血管的血液标本。包括不同年龄和性别的患者。这些样本中,49 例(68.1%)处于稳定状态,其余 23 例(31.9%)处于 VOC 状态。所有样本均进行凝血谱检测。

结果

大多数患者的纤维蛋白原和 D-二聚体水平分别增加了 67%和 71%。与稳定状态相比,患有(VOC)的患者 D-二聚体显著增加(P 值=0.006)。与女性相比,男性的蛋白 S 显著增加,P 值=0.017。凝血酶原时间(PT)、国际标准化比值(INR)和凝血酶时间(TT)结果均在正常范围内。

结论

VOC 期间 D-二聚体水平显著升高,表明凝血和纤维蛋白溶解激活异常。天然抗凝蛋白 C 和 S 的水平降低可作为预测标志物,表明 SCD 患者存在肝损伤。

相似文献

1
Comparative study of hypercoagulability change in steady state and during vaso-occlusive crisis among Sudanese patients living with sickle cell disease.苏丹镰状细胞病患者稳定期与血管阻塞危象期高凝状态变化的对比研究。
Afr Health Sci. 2020 Mar;20(1):392-396. doi: 10.4314/ahs.v20i1.45.
2
Thrombin generation and cell-dependent hypercoagulability in sickle cell disease.在镰状细胞病中凝血酶生成和细胞依赖性高凝状态。
J Thromb Haemost. 2016 Oct;14(10):1941-1952. doi: 10.1111/jth.13416. Epub 2016 Aug 31.
3
Relevance of fibrinolytic protein (D-dimer) and fibrinopeptide A as markers of sickle cell anaemia vaso-occlusive crisis.纤溶蛋白(D - 二聚体)和纤维蛋白肽A作为镰状细胞贫血血管闭塞性危象标志物的相关性
Niger Postgrad Med J. 2014 Sep;21(3):225-30.
4
Thrombophilia in sickle cell disease: the red cell connection.镰状细胞病中的易栓症:红细胞的关联
Blood. 2001 Dec 1;98(12):3228-33. doi: 10.1182/blood.v98.12.3228.
5
Characterization of the hypercoagulable state in patients with sickle cell disease.镰状细胞病患者高凝状态的特征。
Thromb Res. 2012 Nov;130(5):e241-5. doi: 10.1016/j.thromres.2012.08.307. Epub 2012 Sep 7.
6
Thrombin generation reveals high procoagulant potential in the plasma of sickle cell disease children.凝血酶生成揭示镰状细胞病儿童血浆中存在高促凝潜能。
Am J Hematol. 2012 Feb;87(2):145-9. doi: 10.1002/ajh.22206. Epub 2011 Nov 4.
7
Effect of low-dose warfarin on D-dimer levels during sickle cell vaso-occlusive crisis: a brief report.低剂量华法林对镰状细胞血管闭塞性危象期间D-二聚体水平的影响:简要报告
Eur J Haematol. 2004 Mar;72(3):213-6. doi: 10.1111/j.0902-4441.2003.00209.x.
8
Markers of endothelial dysfunction and leucocyte activation in Saudi and non-Saudi haplotypes of sickle cell disease.沙特和非沙特镰状细胞病单倍型中内皮功能障碍和白细胞活化的标志物
Ann Hematol. 2017 Jan;96(1):141-146. doi: 10.1007/s00277-016-2823-7. Epub 2016 Sep 30.
9
Low nitric oxide level is implicated in sickle cell disease and its complications in Ghana.低一氧化氮水平与加纳镰状细胞病及其并发症有关。
Vasc Health Risk Manag. 2018 Sep 6;14:199-204. doi: 10.2147/VHRM.S163228. eCollection 2018.
10
Plasma PTX3 levels in sickle cell disease patients, during vaso occlusion and acute chest syndrome (data from Saudi population).镰状细胞病患者在血管闭塞和急性胸部综合征期间的血浆PTX3水平(来自沙特人群的数据)
Hematology. 2014 Jan;19(1):52-9. doi: 10.1179/1607845413Y.0000000092. Epub 2013 Nov 25.

引用本文的文献

1
Reproductive health issues, infections and non-communicable diseases.生殖健康问题、感染与非传染性疾病。
Afr Health Sci. 2020 Mar;20(1):I-IV. doi: 10.4314/ahs.v20i1.1.

本文引用的文献

1
Sickle cell disease and venous thromboembolism: A retrospective comparison of the rate of positive CT pulmonary angiography in the emergency department.镰状细胞病与静脉血栓栓塞症:急诊行 CT 肺动脉造影阳性率的回顾性比较。
Eur J Radiol. 2019 Jan;110:256-259. doi: 10.1016/j.ejrad.2018.11.033. Epub 2018 Nov 28.
2
The role of carbon monoxide and heme oxygenase in the prevention of sickle cell disease vaso-occlusive crises.一氧化碳和血红素加氧酶在预防镰状细胞病血管闭塞性危象中的作用。
Am J Hematol. 2017 Jun;92(6):569-582. doi: 10.1002/ajh.24750. Epub 2017 Apr 29.
3
Coagulation abnormalities of sickle cell disease: Relationship with clinical outcomes and the effect of disease modifying therapies.镰状细胞病的凝血异常:与临床结局的关系及疾病修饰疗法的影响。
Blood Rev. 2016 Jul;30(4):245-56. doi: 10.1016/j.blre.2015.12.003. Epub 2015 Dec 24.
4
Environmental determinants of severity in sickle cell disease.镰状细胞病严重程度的环境决定因素。
Haematologica. 2015 Sep;100(9):1108-16. doi: 10.3324/haematol.2014.120030.
5
Plasma levels of some coagulation parameters in steady state HBSC disease patients.稳态血红蛋白病患者某些凝血参数的血浆水平。
Pan Afr Med J. 2014 Nov 17;19:289. doi: 10.11604/pamj.2014.19.289.4451. eCollection 2014.
6
Steady state hemoglobin concentration and packed cell volume in homozygous sickle cell disease patients in Lagos, Nigeria.尼日利亚拉各斯纯合子镰状细胞病患者的稳态血红蛋白浓度和红细胞压积
Caspian J Intern Med. 2012 Spring;3(2):405-9.
7
Sickle cell disease in childhood: from newborn screening through transition to adult medical care.儿童镰状细胞病:从新生儿筛查到向成人医疗保健的过渡。
Pediatr Clin North Am. 2013 Dec;60(6):1363-81. doi: 10.1016/j.pcl.2013.09.006.
8
Sickle cell disease and venous thromboembolism: what the anticoagulation expert needs to know.镰状细胞病与静脉血栓栓塞症:抗凝专家须知。
J Thromb Thrombolysis. 2013 Apr;35(3):352-8. doi: 10.1007/s11239-013-0895-y.
9
High D-dimer levels are associated with poor prognosis in cancer patients.高 D-二聚体水平与癌症患者的预后不良相关。
Haematologica. 2012 Aug;97(8):1158-64. doi: 10.3324/haematol.2011.054718. Epub 2012 Feb 27.
10
Sickle cell disease in Middle East Arab countries.中东阿拉伯国家的镰状细胞病。
Indian J Med Res. 2011 Nov;134(5):597-610. doi: 10.4103/0971-5916.90984.